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Nitrile hydratase variant

a nitrile hydratase and nitrile technology, applied in the field of new nitrile hydratase, can solve the problem that there is no attempt to modify the above-mentioned properties, and achieve the effect of improving the enzyme's original activity

Active Publication Date: 2009-09-29
MITSUI CHEM INC
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

The invention provides a nitrile hydratase with a novel mutation site that does not significantly modify its function. The mutation can be introduced into the nitrile hydratase gene by introducing a plasmid containing the gene into a host cell and transforming it with the plasmid. The resulting nitrile hydratase has improved properties such as enzymatic activity, substrate specificity, and stability. The invention also provides a method for modifying the nitrile hydratase by introducing a mutation in the amino acid sequence of the enzyme. The resulting modified nitrile hydratase can be used to produce amide compounds from nitrile compounds. The invention also includes a plasmid containing the gene for nitrile hydratase, a transformant strain containing the plasmid, and a method for producing the nitrile hydratase.

Problems solved by technology

In particular, no attempt has been made regarding the method of modifying the above-mentioned properties by paying attention to the stereostructure of the nitrile hydratase and changing the stereostructure.

Method used

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Examples

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Effect test

reference example 1

Construction (1) of the Substituted Amino Acid Having Nitrile Hydratase Activity

[0210]For the substitution with Met for the 6th Leu in the α-subunit, introduction of site-specific mutation was performed using a “LA PCR in vitro mutagenesis Kit” (manufactured by Takara Shuzo Co., Ltd.). Hereinafter, the “LA PCR in vitro mutagenesis Kit” is simply referred to as the kit. In following Reference Examples, the kit was handled on the basis of the principle thereof and in accordance with the manufacturer's instructions for the kit.

[0211]10 ml of a liquid LB medium was put into a 30 ml test tube, and sterilized by autoclaving at 121° C. for 20 minutes. Ampicillin was added to this medium to have a final concentration of 100 μg / ml. On the medium, one platinum loop of the cells of MT-10822 were inoculated and incubated therein at 37° C. for about 20 hours with stirring at 300 rpm. 1 ml of the resulting culture was put into a suitable centrifugal tube, and this was subjected to centrifugation ...

reference example 2

Construction (2) of the Substituted Amino Acid Having Nitrile Hydratase Activity

[0217]For the substitution with Thr for the 6th Leu in the α-subunit, using the plasmid DNA pPT-DB1 as the template, the plasmid DNA pPT-DB1 was subjected to introduction of site-specific mutation in the same manner as in Reference Example 1.

[0218]Using 10 ng of the plasmid DNA pPT-DB1 as prepared in Reference Example 1 as the template, PCRs of two different types were carried out. For the PCR reaction No. 1, a reaction system of 50 μl in total comprising 50 pmols of the primer having the sequence as forth in SEQ ID No: 11 in the Sequence Listing and 50 pmols of an M13 primer M4 (having the sequence as forth in SEQ ID No: 8 in the Sequence Listing) (for the composition of the system, the manufacturer's instructions for the kit were followed) was used, and the reaction consisted of 25 PCR cycles, in which one PCR cycle comprised thermal denaturation (98° C.) for 15 seconds, annealing (55° C.) for 30 secon...

reference example 3

Construction (3) of the Substituted Amino Acid Having Nitrile Hydratase Activity

[0222]For the substitution with Ala for the 6th Leu in the α-subunit, using the plasmid DNA pPT-DB1 as the template, the plasmid DNA pPT-DB1 was subjected to introduction of site-specific mutation in the same manner as in Reference Example 1.

[0223]Using 10 ng of the plasmid DNA pPT-DB1 as prepared in Reference Example 1 as the template, PCRs of two different types were carried out. For the PCR reaction No. 1, a reaction system of 50 μl in total comprising 50 pmols of the primer having the sequence as forth in SEQ ID No: 12 in the Sequence Listing and 50 pmols of an M13 primer M4 (having the sequence as forth in SEQ ID No: 8 in the Sequence Listing) (for the composition of the system, the manufacturer's instructions for the kit were followed) was used, and the reaction consisted of 25 PCR cycles, in which one PCR cycle comprised thermal denaturation (98° C.) for 15 seconds, annealing (55° C.) for 30 secon...

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Abstract

The amino acid sequence of a mutant which is obtained by introducing a novel mutation into a Pseudonocardia thermophila JCM3095-derived nitrile hydratase consisting of two types of heterogeneous subunits, and the base sequence of the gene are provided. The nitrile hydratase is modified by specifying the region to be modified in the stereostructure / amino acid sequence of the nitrile hydratase, and applying alteration such as substitution, insertion, deletion or the like, to the amino acids in the amino acid sequence which are corresponding to the amino acid residues forming the region. Also provided is a method for modifying an enzyme having a nitrile hydratase activity.

Description

TECHNICAL FIELD[0001]The present invention relates to a novel nitrile hydratase, as well as to a gene encoding the enzyme, to a plasmid containing the gene, to a transformant strain as transformed with the plasmid, to a method for producing a nitrile hydratase using the transformant strain, and to a method for processing a nitrile compound with a culture obtained from cultivating the transformant strain, with the cultivated cells or with a product obtained by processing the cultivated cells, to produce a corresponding amide compound.[0002]Further, the invention relates to a process for modifying the properties of an enzyme having the activity of nitrile hydratase. Furthermore, the invention relates to an enzyme with modified properties, as well as to a gene encoding the enzyme, to a plasmid containing the gene, to a transformant strain transformed with the plasmid, to a method for producing a nitrile hydratase using the transformant strain, and to a method for processing a nitrile c...

Claims

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Application Information

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Patent Type & Authority Patents(United States)
IPC IPC(8): C12N9/88C07K14/00C12N5/10C12N1/21C07H21/00C12Q1/527C12P21/00C12N15/00C12N15/09C12N1/15C12N1/19C12P13/00
CPCC12Y402/01084C12N9/88C12N15/52
Inventor YAMAKI, TOSHIFUMIBANBA, SHINICHIMATOISHI, KAORIITO, KIYOSHIKOBAYASHI, HIDEKITANAKA, EISHIOIKAWA, TOSHIHIRO
Owner MITSUI CHEM INC
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